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Synthesis, Cytotoxicity and Mechanistic Evaluation of 4-Oxoquinoline-3-carboxamide Derivatives: Finding New Potential Anticancer Drugs

As part of a continuing search for new potential anticancer candidates, we describe the synthesis, cytotoxicity and mechanistic evaluation of a series of 4-oxoquinoline-3-carboxamide derivatives as novel anticancer agents. The inhibitory activity of compounds 10–18 was determined against three cance...

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Autores principales: Forezi, Luana da S. M., Tolentino, Nathalia M. C., de Souza, Alessandra M. T., Castro, Helena C., Montenegro, Raquel C., Dantas, Rafael F., Oliveira, Maria E. I. M., Silva, Floriano P., Barreto, Leilane H., Burbano, Rommel M. R., Abrahim-Vieira, Bárbara, de Oliveira, Riethe, Ferreira, Vitor F., Cunha, Anna C., Boechat, Fernanda da C. S., de Souza, Maria Cecília B. V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271384/
https://www.ncbi.nlm.nih.gov/pubmed/24858098
http://dx.doi.org/10.3390/molecules19056651
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author Forezi, Luana da S. M.
Tolentino, Nathalia M. C.
de Souza, Alessandra M. T.
Castro, Helena C.
Montenegro, Raquel C.
Dantas, Rafael F.
Oliveira, Maria E. I. M.
Silva, Floriano P.
Barreto, Leilane H.
Burbano, Rommel M. R.
Abrahim-Vieira, Bárbara
de Oliveira, Riethe
Ferreira, Vitor F.
Cunha, Anna C.
Boechat, Fernanda da C. S.
de Souza, Maria Cecília B. V.
author_facet Forezi, Luana da S. M.
Tolentino, Nathalia M. C.
de Souza, Alessandra M. T.
Castro, Helena C.
Montenegro, Raquel C.
Dantas, Rafael F.
Oliveira, Maria E. I. M.
Silva, Floriano P.
Barreto, Leilane H.
Burbano, Rommel M. R.
Abrahim-Vieira, Bárbara
de Oliveira, Riethe
Ferreira, Vitor F.
Cunha, Anna C.
Boechat, Fernanda da C. S.
de Souza, Maria Cecília B. V.
author_sort Forezi, Luana da S. M.
collection PubMed
description As part of a continuing search for new potential anticancer candidates, we describe the synthesis, cytotoxicity and mechanistic evaluation of a series of 4-oxoquinoline-3-carboxamide derivatives as novel anticancer agents. The inhibitory activity of compounds 10–18 was determined against three cancer cell lines using the MTT colorimetric assay. The screening revealed that derivatives 16b and 17b exhibited significant cytotoxic activity against the gastric cancer cell line but was not active against a normal cell line, in contrast to doxorubicin, a standard chemotherapeutic drug in clinical use. Interestingly, no hemolytical activity was observed when the toxicity of 16b and 17b was tested against blood cells. The in silico and in vitro mechanistic evaluation indicated the potential of 16b as a lead for the development of novel anticancer agents against gastric cancer cells.
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spelling pubmed-62713842018-12-21 Synthesis, Cytotoxicity and Mechanistic Evaluation of 4-Oxoquinoline-3-carboxamide Derivatives: Finding New Potential Anticancer Drugs Forezi, Luana da S. M. Tolentino, Nathalia M. C. de Souza, Alessandra M. T. Castro, Helena C. Montenegro, Raquel C. Dantas, Rafael F. Oliveira, Maria E. I. M. Silva, Floriano P. Barreto, Leilane H. Burbano, Rommel M. R. Abrahim-Vieira, Bárbara de Oliveira, Riethe Ferreira, Vitor F. Cunha, Anna C. Boechat, Fernanda da C. S. de Souza, Maria Cecília B. V. Molecules Article As part of a continuing search for new potential anticancer candidates, we describe the synthesis, cytotoxicity and mechanistic evaluation of a series of 4-oxoquinoline-3-carboxamide derivatives as novel anticancer agents. The inhibitory activity of compounds 10–18 was determined against three cancer cell lines using the MTT colorimetric assay. The screening revealed that derivatives 16b and 17b exhibited significant cytotoxic activity against the gastric cancer cell line but was not active against a normal cell line, in contrast to doxorubicin, a standard chemotherapeutic drug in clinical use. Interestingly, no hemolytical activity was observed when the toxicity of 16b and 17b was tested against blood cells. The in silico and in vitro mechanistic evaluation indicated the potential of 16b as a lead for the development of novel anticancer agents against gastric cancer cells. MDPI 2014-05-22 /pmc/articles/PMC6271384/ /pubmed/24858098 http://dx.doi.org/10.3390/molecules19056651 Text en © 2014 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Forezi, Luana da S. M.
Tolentino, Nathalia M. C.
de Souza, Alessandra M. T.
Castro, Helena C.
Montenegro, Raquel C.
Dantas, Rafael F.
Oliveira, Maria E. I. M.
Silva, Floriano P.
Barreto, Leilane H.
Burbano, Rommel M. R.
Abrahim-Vieira, Bárbara
de Oliveira, Riethe
Ferreira, Vitor F.
Cunha, Anna C.
Boechat, Fernanda da C. S.
de Souza, Maria Cecília B. V.
Synthesis, Cytotoxicity and Mechanistic Evaluation of 4-Oxoquinoline-3-carboxamide Derivatives: Finding New Potential Anticancer Drugs
title Synthesis, Cytotoxicity and Mechanistic Evaluation of 4-Oxoquinoline-3-carboxamide Derivatives: Finding New Potential Anticancer Drugs
title_full Synthesis, Cytotoxicity and Mechanistic Evaluation of 4-Oxoquinoline-3-carboxamide Derivatives: Finding New Potential Anticancer Drugs
title_fullStr Synthesis, Cytotoxicity and Mechanistic Evaluation of 4-Oxoquinoline-3-carboxamide Derivatives: Finding New Potential Anticancer Drugs
title_full_unstemmed Synthesis, Cytotoxicity and Mechanistic Evaluation of 4-Oxoquinoline-3-carboxamide Derivatives: Finding New Potential Anticancer Drugs
title_short Synthesis, Cytotoxicity and Mechanistic Evaluation of 4-Oxoquinoline-3-carboxamide Derivatives: Finding New Potential Anticancer Drugs
title_sort synthesis, cytotoxicity and mechanistic evaluation of 4-oxoquinoline-3-carboxamide derivatives: finding new potential anticancer drugs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271384/
https://www.ncbi.nlm.nih.gov/pubmed/24858098
http://dx.doi.org/10.3390/molecules19056651
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